<< Back To Search

A Study of JNJ-79635322 in Participants With Relapsed or Refractory Multiple Myeloma or Previously Treated Amyloid Light-chain (AL) Amyloidosis

Notify the Multiple Myeloma Research Foundation you are interested in this trial
NCT05652335
Age 18 +
Sex Both
Phase Phase 1
Third Opinion Trial Synopsis
In this clinical study, researchers are exploring a new treatment approach for patients with a specific type of blood cancer. The study focuses on using a combination of therapies to improve patient outcomes. Here are some key points about the study:
  • The treatment involves a unique combination of existing therapies that have shown promise in previous studies.
  • Patients will receive the treatment in a specific sequence, which is designed to maximize effectiveness.
  • The study aims to evaluate how well this combination works compared to standard treatments.
  • Researchers are also looking at the safety of the treatment and any side effects that may occur.
  • This study is being conducted at multiple centers, allowing for a diverse group of participants.
  • Patients will be closely monitored throughout the study to track their progress and response to the treatment.
Overall, this study is significant because it seeks to improve treatment options for patients by combining therapies in a new way, potentially leading to better outcomes and quality of life.
Third Opinion AI Generated Synopsis

Trial Summary
The primary purpose of this study is to identify the recommended phase 2 dose (RP2D\[s\]) and schedule(s) to be safe for JNJ-79635322 in Part 1 (dose escalation), and to characterize the safety and tolerability of JNJ-79635322 at the RP2D(s) selected and in disease subgroups in Part 2 (dose expansion).
from ClinicalTrials.gov

Locations & Contact

Fill out the form and to let the Multiple Myeloma Research Foundation know you are interested in this trial.

Please share any additional considerations or concerns:
Example: Are you newly diagnosed? What treatments have you already been on?

Contacts: